D'Agostino Marcelo, Marti Myrna, Mejía Felipe, de Cosio Gerardo, Faba Gladys
Unidad de Análisis e Información en Salud, Departamento de Enfermedades Transmisibles y Análisis de Salud Organización Panamericana de la Salud/Organización Mundial de la Salud Washington D.C Estados Unidos de América Unidad de Análisis e Información en Salud, Departamento de Enfermedades Transmisibles y Análisis de Salud, Organización Panamericana de la Salud/Organización Mundial de la Salud, Washington D.C., Estados Unidos de América.
Oficina de Gestión del Conocimiento, Bioética e Investigación Organización Panamericana de la Salud/Organización Mundial de la Salud Buenos Aires Argentina Oficina de Gestión del Conocimiento, Bioética e Investigación, Organización Panamericana de la Salud/Organización Mundial de la Salud, Buenos Aires, Argentina.
Rev Panam Salud Publica. 2017 Mar 23;41:e27. doi: 10.26633/RPSP.2017.27. eCollection 2017.
Policy development and review, planning, innovation, research, and the measurement of progress, barriers, and opportunities require open access to reliable data, information, and expert knowledge. This is part of the principles of the Pan American Sanitary Code and the Constitution of the Pan American Health Organization. Between 1950 and 1978, the subject of health data collection, in particular vital statistics, was expressly addressed in each of the first seven editions of Health in the Americas. However, despite considerable improvement in data quality, since the early 1980s it has been recognized that countries' health information systems require constant modernization in order to provide health data with better quality, coverage, and timeliness for informed decision-making. With the rise of the Internet, growing access to information and communications technologies--and today, with social networks, the increase in available content--has become massive and is growing in an exponential, unstructured, unclassified, and often uncontrolled manner. This situation forces health institutions to adopt strategies and standards for the management of open data that make it possible to strengthen their quality, confidentiality, and security. We propose a strategy for the governance of health data using tools, concepts, and recommendations that will enable countries to generate open, higher-quality, reliable, and secure data.
政策制定与审查、规划、创新、研究以及对进展、障碍和机遇的衡量,都需要能够公开获取可靠的数据、信息和专家知识。这是《泛美卫生法典》和泛美卫生组织章程原则的一部分。1950年至1978年期间,《美洲卫生状况》的前七版均明确提及了卫生数据收集主题,尤其是生命统计数据。然而,尽管数据质量有了显著提高,但自20世纪80年代初以来,人们认识到各国的卫生信息系统需要不断现代化,以便提供质量更高、覆盖范围更广且更及时的卫生数据,用于明智决策。随着互联网的兴起,信息和通信技术的获取日益增加,如今,借助社交网络,可用内容的增长已变得十分庞大,且呈指数级增长,具有非结构化、未分类且往往不受控制的特点。这种情况迫使卫生机构采用开放数据管理的策略和标准,以提高数据的质量、保密性和安全性。我们提出了一项利用工具、概念和建议对卫生数据进行治理的策略,这将使各国能够生成开放、高质量、可靠且安全的数据。